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Lumbar Puncture

Essentials

  • An emergency sample of cerebrospinal fluid is most often taken when acute central nervous system infection or polyradiculitis is suspected, or to exclude subarachnoid haemorrhage (SAH) if cranial CT is normal.
  • A non-emergency sample is most often taken when central nervous system inflammation, such as MS, neurosarcoidosis or neuroborreliosis, is suspected, as well as in some cases of suspected malignancy.
  • Before the procedure, check the ocular fundi to make sure that the optic discs are clearly defined. This signifies normal intracranial pressure and safe puncture.
  • The procedure is performed in the lumbar spine area, where there is no spinal cord but a cavity filled with cerebrospinal fluid. This, as well as the course of events, should be explained to the patient beforehand.
  • Careful positioning of the patient in the correct position for the procedure is most important for successful lumbar puncture. Sufficient time should be taken for ensuring the correct position.
  • Bed rest after lumbar puncture does not prevent post lumbar puncture headache. Should such headache be prolonged, it should primarily be treated by intravenous caffeine infusion in hospital.

Performance of lumbar puncture

Therapy affecting blood coagulation

  • Before the puncture, check complete blood count, prothrombin time and APTT, unless these have been determined within the previous 6 months.
  • The platelet count should be > 50 × 109 /l.
  • Antithrombotic therapy and lumbar puncture
    • ASA therapy used for secondary prevention does not need to be withheld; if it is used for primary prevention, it is withheld 5-7 days before the puncture.
    • ASA-dipyridamole therapy: last tablet in the previous evening before the puncture and the next tablet in the next morning after the puncture day.
    • Clopidogrel therapy is generally not withheld, unless there are other factors affecting the bleeding tendency.
  • Make sure to ask about any anticoagulant therapy before the procedure.
    • Warfarin treatment must be withheld 2-4 days before the puncture.
    • Bridge therapy is not required for low-risk patients (e.g. atrial fibrillation without another cardiac disease)
    • Subcutaneous low-molecular-weight heparin (LMWH) is started as bridge therapy for high-risk patients (e.g. prosthetic mitral valve, severe thrombophilia, recent thrombosis).
      • Enoxaparin 0.5 mg/kg twice daily or dalteparin 50 IU/kg twice daily
      • The last LMWH injection is administered 18-24 hours before the puncture (this also applies to patients who are on LMWH for some other reason).
      • INR is checked on the morning of the day when the puncture is to be performed. INR level < 1.5 is safe.
      • LMWH therapy is resumed no earlier than 6 hours after the lumbar puncture, at the same time with warfarin therapy that is started using earlier home dosage, and continued until INR level has been within therapeutic range for two consecutive days.
    • Before emergency lumbar puncture the effect of warfarin must be reversed.
    • A 1- to 2-day break is recommended for the direct oral anticoagulants (DOACs, 2 days if bleeding risk is pronounced).
      • Resumed not earlier than the following morning.

Carrying out the lumbar puncture

  • If the patient has undergone cranial imaging just before the procedure showing normal intracranial pressure, inspection of the ocular fundi is not necessary. If this is not the case, the inspection must always be performed.
  • Check the patient's position carefully before the procedure; the aim is to have the back as curved as possible so as to have the intervertebral spaces open. If necessary, ask assisting personnel to keep the patient in the correct position during puncture. The most common error is to have the spine twisted instead of only being bent forward.
  • Lumbar puncture can be performed with the patient lying on his/her side or in the sitting position if there is no need to measure the opening pressure. The opening pressure can only be measured with the patient lying on his/her side. If a sample cannot be obtained in one position, an attempt can be made in the other, and this often helps.
  • Before scrubbing, palpate the anterior superior iliac spine carefully. Get a clear picture of the spatial configuration of the patient's spine, and identify the best place to insert the needle. Mark the entry site with your nail or with a pen.
  • Local anaesthesia removes the sensation of pain on the skin surface and may calm the patient. However, it is not absolutely necessary because two needle pricks will then be needed and local anaesthesia will not remove the sensation of pain in deeper tissues. It is forbidden to anaesthetize the deeper tissue layers as the anaesthetic may enter the spinal cavity.
  • If possible, avoid inserting the needle through a scar because a scar will be difficult to penetrate.
  • Insertion through a tattoo or other abnormal skin area is not recommended, either.
  • The procedure is normally performed in the intervertebral space either above (L3-L4) or below (L4-L5) the level of the anterior superior iliac spine. Direct the needle diagonally upward, taking note of the anatomic "landmarks" you feel (and also any sharp sensation experienced by the patient in a lower limb). When pressure against the needle tip decreases, you have probably reached the right place.
  • The procedure may be technically impossible to perform if the patient is very obese, has a history of lumbar fusions or has severe spinal stenosis.
  • If the patient is discharged soon after the lumbar puncture, he/she must be informed about possible postpuncture headache and how to treat it.
  • The time of the lumbar puncture and its performance need to be documented in the medical records as well as any problems and peripheral blood contamination, as the latter may lead to a suspicion of SAH and consequent unnecessary procedures.

Post lumbar puncture headache

  • Occurs in about 10% of patients after sampling and is probably caused by loss of CSF pressure.
  • The headache typically occurs only in the upright position and is alleviated by lying down.
  • The onset of headache is related more to the amount of fluid leaking into tissues after the puncture than to the amount of fluid withdrawn as a sample. Bed rest after puncture does not prevent headache Posture and Fluids for Preventing Post-Dural Puncture Headache, but strenuous exercise should be avoided for a couple of days.
  • Drinking of coffee apparently does not prevent post lumbar puncture headache.

Treatment

  • Bed rest is generally all that is needed. Sick leave is necessary for about 3 days.
  • Analgesics are fairly ineffective.
  • For nausea, prochlorperazine is suitable.
  • Two consecutive intravenous caffeine infusions are normally given in hospital Drug Therapy for Treating Post-Dural Puncture Headache before the application of a blood patch, which is the most effective treatment for postpuncture headache Epidural Blood Patching for Post-Dural Puncture Headache.
  • Blood patch
    • Consult an anaesthesiologist if severe headache persists for more than 3 days.
    • The patient's own blood is injected into the area around the puncture site.
    • This procedure requires sterile operating-room conditions and is generally effective.

CSF analysis

  • Cerebrospinal fluid is normally colourless and clear.
  • Turbid, opaque CSF suggests bacterial meningitis.
  • Evenly bloody, watery CSF ("lingonberry juice"), reddish/yellow-red after centrifugation (xanthochromia), suggests haemorrhage.
  • Yellowish CSF suggests a high protein concentration.
  • Fluid that is coagulated and streaked with blood or bloody but later clear and after centrifugation colourless suggests peripheral blood contamination.
  • The most common CSF findings are listed in table T1.

Most common CSF findings

Normal CSFAbnormal findingOther information
Erythrocytes0
0-1 000
- Mildly haemorrhagic disturbance (infarction, encephalitis, etc.)
1 000-100 000
- Haemorrhage (cerebral haemorrhage, SAH)
1-1 000 often an artefact
Leucocytes0-3/mm3
4-100/mm3
- MS
- Neuroborreliosis
- Neurosarcoidosis
- Viral, tuberculous or fungal meningitis
- Neurosyphilis
- Autoimmune/paraneoplastic encephalitis
- Neurolymphoma, neuroleukaemia
- Meningeal carcinomatosis
- Cerebral vasculitis
- Meningeal irritation from general infection
100-1 000/mm3
- Viral meningitis or other serous meningitis
- Tuberculous meningitis
- Listeria meningitis
- Old haemorrhage?
>1 000 mm3
- Bacterial meningitis
Laboratories state the percentages of polymorphonuclear and mononuclear leucocytes.
In the cell count, malignant cells can be interpreted as leucocytes. Their accurate interpretation requires microscopic analysis.
In samples with peripheral blood contamination there is about 1 leucocyte / 1 000 erythrocytes.
All diseases listed here, with the exception of bacterial meningitis, cause mononuclear pleocytosis
Glucose2.2-4.2 mmol/l (about half of blood glucose level)
Increased: diabetes, glucose infusion
Decreased: infection (bacteria, tuberculosis, fungus), neurosarcoidosis
Check blood glucose at the time of puncture
Protein150-450 mg/l
Decreased: no practical implications
Increased:
- Haemorrhage, tumours, polyradiculitis, meningitis, encephalitis, disturbance in the circulation of CSF, several neurodegenerative diseases
- High blood protein concentration (e.g. myeloma, tuberculosis)
- Damage of the blood-brain barrier (e.g. CSF blockage)
- Increased CNS antibody synthesis (e.g. MS)
- Diabetes
- In the elderly, protein concentration can be increased without pathology.
Oligoclonal IgG-bands: in about 90% of MS-patients, in chronic infections or as sequela of certain infections

Other CSF tests

  • IgG index and oligoclonal bands: if MS is suspected Multiple Sclerosis (Ms)
  • ACE: if neurosarcoidosis is suspected Sarcoidosis
  • Borrelia antibodies and chemokine CXCL 13: in case of suspected borreliosis if serum Borrelia antibodies are increased Lyme Borreliosis (LB) and often if CNS inflammation or infection is suspected
  • TPHA and FTA absorption: if neurosyphilis is suspected Syphilis
  • Lactate: if infection is suspected; also increased in cerebrovascular disorders, traumas and in connection with convulsions, nowadays rarely used

Exfoliated cells in CSF (microscopic analysis)

  • Provides somewhat varying information depending on the laboratory technique used.
  • Findings
    • Malignant cells are found in meningeal carcinomatosis (several samples may be required) and in CNS leukaemia, but rarely in connection with primary brain neoplasms.
    • Plasma cells strongly suggest MS; a more common finding in MS is the so-called lymphoid reaction.
    • In connection with CNS infections, independent of the cause, there are three phases in the cellular presentation of CSF:
      • neutrophilic or exudative phase
      • lymphocytic or proliferative phase
      • mononuclear or phagocytic phase.

Emergency examination of CSF

Indications

  • Bacterial meningitis (absolutely necessary; see Meningitis in Adults)
    • In patients with suspected bacterial meningitis, lumbar puncture should be performed before cranial imaging. A delay in the performance of CSF examination must not cause delay in the commencement of antimicrobial treatment.
  • Encephalitis Encephalitis
  • Sometimes viral meningitis Meningitis in Adults
    • If the symptoms and findings are completely typical, sampling is not necessary because it will not affect further treatment.
  • Cranial CT is the primary diagnostic procedure for SAH. Lumbar puncture is indicated if the symptoms started more than 6 hours ago, the cranial CT is normal and there is a clinical possibility of SAH (5% of cases) because a normal finding on brain CT does not rule out SAH.
    • In suspected SAH, the rule of halves in CSF examination dictates that:
      • erythrocytes appear in CSF in half an hour
      • xanthochromia, i.e. yellowness of the sample (caused by bilirubin), appears in CSF in half a day
      • erythrocytes disappear from CSF in half a week
      • xanthochromia disappears from CSF in half a month (in 2 weeks).
    • In the spectral analysis of the CSF primarily bilirubin is determined. The sensitivity of the test is 100% within 12 hours to 2 weeks after SAH and still 40-70% 4 weeks after SAH.
  • Polyradiculitis: high protein concentration is the earliest diagnostic finding.

Contraindications

  • Focal neurological signs when imaging has not been performed.
  • Suspected increased intracranial pressure (risk of cerebellar herniation!)
  • In unclear situations, if proper view of the ocular fundi cannot be obtained, CT of the head is indicated before lumbar puncture.

Relative contraindications

  • Anticoagulant therapy or bleeding tendency of other origin (see above)

Other considerations

  • If meningitis is suspected, culture the sample in a dish (procure the necessary dish in advance) or, in case of emergency, in a blood culture bottle, and keep part of the sample for bacterial staining.
  • Take an extra tube of CSF to be stored in the laboratory refrigerator for possible further tests.